Rad51p and Rad54p, but not Rad52p, elevate gene repair in Saccharomyces cerevisiae directed by modified single-stranded oligonucleotide vectors

被引:62
作者
Liu, L
Cheng, SQ
van Brabant, AJ
Kmiec, EB
机构
[1] Univ Delaware, Delaware Biotechnol Inst, Dept Biol, Newark, DE 19711 USA
[2] NaPro Genom, Newark, DE 19711 USA
关键词
D O I
10.1093/nar/gkf397
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Synthetic single-stranded DNA vectors have been used to correct point and frameshift mutations in episomal or chromosomal targets in the yeast Saccharomyces cerevisiae. Certain parameters, such as the length of the vector and the genetic background of the organism, have a significant impact on the process of targeted gene repair, and point mutations are corrected at a higher frequency than frameshift mutations. Genetic analyses reveal that expression levels of the recombination/repair genes RAD51, RAD52 and RAD54 can affect the frequency of gene repair. Overexpression of RAD51 enhances the frequency 4-fold for correction of an episomal target and 5-fold for correction of a chromosomal target; overexpression of RAD54 is also effective in stimulating gene repair, to the same extent as RAD51 in the chromosomal target. In sharp contrast, RAD52 gene expression serves to reduce gene repair activity in rescue experiments and in experiments where RAD52 is overexpressed in a wild-type strain. This may suggest an antagonist role for Rad52p. Consistent with this notion, the highest level of targeted repair occurs when the RAD51 gene is overexpressed in a strain of yeast deficient in RAD52 gene function.
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收藏
页码:2742 / 2750
页数:9
相关论文
共 38 条
[1]   Stable and inheritable changes in genotype and phenotype of albino melanocytes induced by an RNA-DNA oligonucleotide [J].
Alexeev, V ;
Yoon, K .
NATURE BIOTECHNOLOGY, 1998, 16 (13) :1343-1346
[2]   Localized in vivo genotypic and phenotypic correction of the albino mutation in skin by RNA-DNA oligonucleotide [J].
Alexeev, V ;
Igoucheva, O ;
Domashenko, A ;
Cotsarelis, G ;
Yoon, K .
NATURE BIOTECHNOLOGY, 2000, 18 (01) :43-47
[3]   Enhanced gene transfer into HuH-7 cells and primary rat hepatocytes using targeted liposomes and polyethylenimine [J].
Bandyopadhyay, P ;
Kren, BT ;
Ma, XM ;
Steer, CJ .
BIOTECHNIQUES, 1998, 25 (02) :282-+
[4]   Nucleotide exchange in genomic DNA of rat hepatocytes using RNA/DNA oligonucleotides - Targeted delivery of liposomes and polyethyleneimine to the asialoglycoprotein receptor [J].
Bandyopadhyay, P ;
Ma, XM ;
Linehan-Stieers, C ;
Kren, BT ;
Steer, CJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (15) :10163-10172
[5]   In vivo targeted repair of a point mutation in the canine dystrophin gene by a chimeric RNA/DNA oligonucleotide [J].
Bartlett, RJ ;
Stockinger, S ;
Denis, MM ;
Bartlett, WT ;
Inverardi, L ;
Le, TT ;
Man, NT ;
Morris, GE ;
Bogan, DJ ;
Metcalf-Bogan, J ;
Kornegay, JN .
NATURE BIOTECHNOLOGY, 2000, 18 (06) :615-622
[6]   A tool for functional plant genomics:: Chimeric RNA/DNA oligonucleotides cause in vivo gene-specific mutations [J].
Beetham, PR ;
Kipp, PB ;
Sawycky, XL ;
Arntzen, CJ ;
May, GD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (15) :8774-8778
[7]  
Brachman EE, 2002, CURR OPIN MOL THER, V4, P171
[8]   Correction of the mutation responsible for sickle cell anemia by an RNA-DNA oligonucleotide [J].
ColeStrauss, A ;
Yoon, KG ;
Xiang, YF ;
Byrne, BC ;
Rice, MC ;
Gryn, J ;
Holloman, WK ;
Kmiec, EB .
SCIENCE, 1996, 273 (5280) :1386-1389
[9]   HERITABLE DAMAGE TO YEAST CAUSED BY TRANSFORMATION [J].
DANHASH, N ;
GARDNER, DCJ ;
OLIVER, SG .
BIO-TECHNOLOGY, 1991, 9 (02) :179-182
[10]   EVOLUTION OF THE SNF2 FAMILY OF PROTEINS - SUBFAMILIES WITH DISTINCT SEQUENCES AND FUNCTIONS [J].
EISEN, JA ;
SWEDER, KS ;
HANAWALT, PC .
NUCLEIC ACIDS RESEARCH, 1995, 23 (14) :2715-2723